Canonical Allele Identifier: CA16248555
Gene: WWC1 HGNC NCBI

Linked Data

dbSNP Id: rs10475878

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.168363199G>A , CM000667.2:g.168363199G>A GRCh38
NC_000005.9:g.167790204G>A , CM000667.1:g.167790204G>A GRCh37
NC_000005.8:g.167722782G>A NCBI36
NG_016712.1:g.76140G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000265293.9:c.120-8225G>A MANE Select ENSP00000265293.4:n.120-8225G>A
ENST00000265293.8:c.120-8225G>A ENSP00000265293.4:n.120-8225G>A
ENST00000519859.1:n.186-8225G>A
ENST00000521089.5:c.120-8225G>A ENSP00000427772.1:n.120-8225G>A
ENST00000523043.5:n.27-8225G>A
NM_001161661.1:c.120-8225G>A NP_001155133.1:n.120-8225G>A
NM_001161662.1:c.120-8225G>A NP_001155134.1:n.120-8225G>A
NM_015238.2:c.120-8225G>A NP_056053.1:n.120-8225G>A
XM_005265850.1:c.120-8225G>A XP_005265907.1:n.120-8225G>A
XM_005265853.1:c.120-8225G>A XP_005265910.1:n.120-8225G>A
XM_011534485.1:c.120-8225G>A XP_011532787.1:n.120-8225G>A
XM_011534486.1:c.120-8225G>A XP_011532788.1:n.120-8225G>A
XM_011534487.1:c.120-8225G>A XP_011532789.1:n.120-8225G>A
XM_011534488.1:c.120-8225G>A XP_011532790.1:n.120-8225G>A
XM_011534489.1:c.120-8225G>A XP_011532791.1:n.120-8225G>A
XM_011534490.1:c.120-8225G>A XP_011532792.1:n.120-8225G>A
XM_011534491.1:c.120-8225G>A XP_011532793.1:n.120-8225G>A
XM_005265853.2:c.120-8225G>A XP_005265910.1:n.120-8225G>A
XM_017009276.1:c.120-8225G>A XP_016864765.1:n.120-8225G>A
XM_017009278.1:c.-235-8225G>A XP_016864767.1:n.-235-8225G>A
NM_001161661.2:c.120-8225G>A NP_001155133.1:n.120-8225G>A
NM_001161662.2:c.120-8225G>A NP_001155134.1:n.120-8225G>A
NM_015238.3:c.120-8225G>A MANE Select NP_056053.1:n.120-8225G>A